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Analyst, QC I
Ref No.: 18-13035
Location: Novato, California
Effective performance ensures that the Quality Control department and the company achieve the annual objectives with respect to the established goals and budget. An effective Analyst will perform routine assays so that the effort of other personnel can be applied to non-routine situations or assays that require special attention. The Analyst will begin to apply his/her skills to non-routine samples which may include: process development and validation samples/studies. In addition, the support functions of the Analyst position maintains the laboratory in a productive and compliant state, further optimizing the utilization of all personnel resources. The Analyst is expected to spend between 80-90% of his/her time in the laboratory and complete all test records associated with testing when the assay is complete. Test records are expected to be completed in 1-2 business days and turned over for review. If a test does not meet system suitability requirements, the analyst is expected to notify his/her supervisor within one business day so an investigation may be opened in a timely manner.

At least one year in a cGMP/GLP laboratory; quality control experience is preferred.
Ability to follow written instructions and to perform tasks with direct or minimal supervision.
Familiarity with use of a computer; e.g., Proficient in Windows, Microsoft Word, Excel, LIMS.
Viral/ gene therapy work experience is preferred but not required.
Good written, verbal, and communication skills.
Good documentation skills.
Demonstrates the ability to work independently.